US4338375A - Surface coating composition - Google Patents

Surface coating composition Download PDF

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Publication number
US4338375A
US4338375A US06/153,242 US15324280A US4338375A US 4338375 A US4338375 A US 4338375A US 15324280 A US15324280 A US 15324280A US 4338375 A US4338375 A US 4338375A
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weight
coating composition
coating
group
parts
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US06/153,242
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English (en)
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Kaname Hashimoto
Saizo Ikeda
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Daicel Corp
ITT Inc
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Daicel Chemical Industries Ltd
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04—Polysiloxanes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31507—Of polycarbonate
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31609—Particulate metal or metal compound-containing
    • Y10T428/31612—As silicone, silane or siloxane
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31652—Of asbestos
    • Y10T428/31663—As siloxane, silicone or silane

Definitions

  • This invention relates to a surface coating composition capable of providing an abrasion resistant surface, and particularly to a surface coating composition which can be coated and hardened on the surface of a plastic material and which possesses excellent transparency, abrasion resistance, heat resistance, adhesion to the base material and water resistance.
  • Plastic materials have been applied to a variety of uses due to their desirable characteristics such as high impact resistance, easy moldability and light weight. However, they have the drawback that the surface of a molded plastic material is apt easily to be scratched. Accordingly, it has been proposed to form a hardened coating of an organopolysiloxane resin on the surface of a molded plastic material for the purpose of improving the abrasion resistant property of the surface of the plastic material.
  • a coating solution comprising an organo-polysiloxane that can be hardened by reaction and a hardening catalyst is coated on the surface of a plastic material and is hardened by heating to form a hardened coating having a good abrasion resistant property as disclosed in, for example, Japanese Provisional Patent Publication No. 50(1975)-143,822.
  • a coating produced simply by cross-linking the organopolysiloxane to a higher level by the use of a hardening catalyst has a poor sliding property, due to its high friction coefficient. Therefore, it is important to improve the poor sliding property by producing a smoother coated surface so as to provide an improved abrasion resistant property.
  • a surface active agent as a leveling agent to provide a smooth coated surface. Nevertheless, conventional surface active agents do not provide a satisfactory leveling effect to a coating solution containing an organopolysiloxane.
  • the adhesion property of the coating composition to the base material is apt to decrease, the coated film is apt to be made opaque due to the poor solubility of the surface active agent in the organopolysiloxane, or pinholes may be produced in the film surface when the film is immersed in water.
  • the last defect is caused by the incorporated surface active agent being dissolved in the water so that it escapes from the film.
  • a fully satisfactory surface active agent for this specific purpose is not known.
  • the coated material is brought into contact with an alkaline hardening catalyst after being dried. Since the hardening time of organopolysiloxane coatings is much longer than is required for general coating materials, the surface active agent should have improved acid resistance, alkali resistance and heat resistance. However, a surface active agent fully satisfying these requirements is not known.
  • the present invention accordingly, is a surface coating composition
  • a surface coating composition comprising:
  • R 1 represents an aliphatic hydrocarbon group of C 1 -C 4 or an aromatic hydrocarbon group
  • R 2 represents an aliphatic hydrocarbon group of C 1 -C 4 ;
  • the surface coating composition of the invention is dissolved in a solvent, such as an alcohol, to obtain a coating solution.
  • a hardening catalyst can be added to the coating solution.
  • the thus-obtained coating solution is coated on the surface of a material, such as plastic material, metal, wood, glass, etc., and is hardened by drying to give a surface film having an excellent abrasion resistant property.
  • a material such as plastic material, metal, wood, glass, etc.
  • the produced surface film is excellent in transparency, abrasion resistant property, heat resistance, adhesion to the base material, water resistance, surface smoothness and friction resistance.
  • the organotrialkoxysilane of the present invention is represented by the general formula R 1 Si(OR 2 ) 3 , in which R 1 is an aliphatic hydrocarbon group of C 1 -C 4 , such as methyl, ethyl, propyl or butyl, or an aromatic hydrocarbon group such as phenyl or tolyl, and R 2 is an aliphatic hydrocarbon group of C 1 -C 4 , such as methyl, ethyl, propyl or butyl.
  • R 1 is an aliphatic hydrocarbon group of C 1 -C 4 , such as methyl, ethyl, propyl or butyl, or an aromatic hydrocarbon group such as phenyl or tolyl
  • R 2 is an aliphatic hydrocarbon group of C 1 -C 4 , such as methyl, ethyl, propyl or butyl.
  • a typical organotrialkoxysilane is exemplified by methyltriethoxys
  • the partially hydrolyzed condensation product of the organotrialkoxysilane is an initially hydrolyzed condensation product which can be obtained by adding water and a small amount of an acid to the organotrialkoxysilane, and heating same for 1-10 hours at a temperature of 50°-80° C., as stated, for example, in U.S. Pat. No. 3,451,838.
  • a partially hydrolyzed copolycondensation product of the above-mentioned organotrialkoxysilane with a tetraalkoxysilane can be employed in order to improve the hardness of the coated film.
  • the tetraalkoxysilane is represented by Si(OR 3 ) 4 , in which R 3 is an aliphatic hydrocarbon group of C 1 -C 6 , such as tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane or tetrabutoxysilane.
  • the amount of the tetraalkoxysilane is not more than 40% by weight based on the total amount of the organotrialkoxysilane and tetraalkoxysilane.
  • a mixture of the respective partially hydrolyzed condensation products of an organotrialkoxysilane and a tetraalkoxysilane can be employed.
  • the partially hydrolyzed condensation product of an organotrialkoxysilane is preferably used in the form of a solution in an alkyl alcohol of C 1 -C 4 , preferably ethyl alcohol.
  • the organic carboxylic acid of C 1 -C 5 is exemplified by formic acid, acetic acid, propionic acid, valeric acid, pivalic acid and thioacetic acid.
  • the organic carboxylic acid is added to lengthen the pot life of the coating solution and further to improve the adhesion of the coated film.
  • the kind and the amount of the organic carboxylic acid can be selected depending on the coating purpose, coating conditions and hardening conditions.
  • the organic carboxylic acid is generally employed in an amount ranging from 10 to 100 parts by weight, preferably from 60 to 70 parts by weight, per 100 parts of the partially hydrolyzed condensation product of the organotrialkoxysilane.
  • the hardening catalyst which can be employed in the composition according to the invention, if desired, can be an inorganic or organic alkaline compound effective for hardening the organopolysiloxane.
  • the hardening catalyst include sodium phosphate, sodium borate, sodium azide, sodium naphthenate, tetrasodium salt of ethylenediaminetetraacetic acid (EDTA), triethylamine, 1,8-diazabicyclo-(5.4.0)undecane-7, 1,5-diazabicyclo(4.3.0)nonene-5, and tetraethylammonium hydroxide.
  • the hardening catalyst can be incorporated in an amount that varies depending on the selected temperature and time for the hardening. Accordingly, there is no critical limitation on the amount, but an amount ranging from 0.01 to 10 parts by weight, per 100 parts by weight of the partially hydrolyzed condensation product of the organotrialkoxysilane, can be employed.
  • the anionic surface active agent containing a fluorocarbon chain employed in the composition according to the invention, is represented by the formula R f A, in which R f is a fluorinated aliphatic hydrocarbon group, a part or all of the hydrogen atoms of the aliphatic hydrocarbon chain being replaced with fluorine atoms, and A is an anionic functional group stably combined with the R f group.
  • R f and A can be directly coupled to each other to form R f A, or they can be stably coupled to each other by means of an appropriate coupling group such as an alkylene group or --OR--, as represented by R f -R-A, R f -O-R-A or ##STR1## in which R is a divalent aliphatic hydrocarbon group, n is an integer from 1 to 3 and O is an oxygen atom.
  • R f is a group derived from an oligomer of perfluoro-propylene in which 2 to 6 monomers are contained.
  • the trimer is especially preferable.
  • the oligomer is very effective because it has a low surface tension due to the function of the side chain of CF 3 .
  • the carbon atom number of the group R f preferably is in the range from 1 to 20 and particularly preferred is a carbon atom number in the range from 6 to 11.
  • R f can be a straight or branched chain, and it can contain a double bond in the structure, i.e. the aliphatic hydrocarbon can be alkyl or alkenyl.
  • A is an anionic functional group such as --SO 3 H, --SO 3 Na, --SO 3 K, --COOH, --COONa, and --COOK.
  • anionic surface active agent containing a fluorocarbon chain examples include:
  • the fluorocarbon-type surface active agent is preferably incorporated in an amount ranging from 0.01 to 1.0 part by weight per 100 parts by weight of the partially hydrolyzed condensation product of the organotrialkoxysilane.
  • An amount less than 0.01 part cannot provide satisfactory surface smoothness and abrasion resistant property.
  • An amount more than 1.0 part is also unsuitable, because such a large amount cannot bring about a satisfactory surface adhesion of the hardened coated film.
  • composition of the invention is used in the form of a coating solution in a solvent such as an alcohol, ketone or ester.
  • a solvent such as an alcohol, ketone or ester.
  • An appropriate solvent can be selected from a variety of solvents such as an alcohol solvent, a ketone solvent, an ester solvent, a low boiling solvent, a medium boiling solvent and a high boiling solvent, depending on the kind of a material to be coated and the coating conditions.
  • Additives such as an ultra-violet absorber, an anti-oxidizing agent, an inorganic material powder, etc., can be additionally incorporated into the coating solution, if desired.
  • the coating procedure examples include the dipping process, the spraying process, the flow coating process and the spin coating process. Any process can be employed to provide a smooth-faced, hardened, coated film and to give the full effect of the fluorocarbon-type surface active agent incorporated in the solution.
  • the coating solution prepared as above is advantageously applied particularly to a base material which is a molded plastic material having an inferior abrasion resistant property.
  • plastic material to which the coating solution can be applied examples include transparent plastic materials such as polymethylmethacrylate, polycarbonate, polystyrene, acrylonitrile-styrene copolymer, methyl methacrylate-styrene copolymer, polydiethyleneglycol bisallylcarbonate, a transparent ABS resin, a rubber-reinforced methacrylic resin, cellulose acetate, cellulose acetate propionate, cellulose acetate butyrate, and polyvinyl chloride, and opaque plastic materials such as an ABS resin and high-impact polystyrene.
  • transparent plastic materials such as polymethylmethacrylate, polycarbonate, polystyrene, acrylonitrile-styrene copolymer, methyl methacrylate-styrene copolymer, polydiethyleneglycol bisallylcarbonate, a transparent ABS resin, a rubber-reinforced methacrylic resin, cellulose acetate, cellulose a
  • the coated plastic material is subjected to the drying and hardening process at a temperature below the thermal deformation temperature of the molded plastic material.
  • the hardening temperature employed varies with the nature of the plastic material that is employed. Generally, the temperature ranges from 40° to 140° C., and preferably ranges from 80° to 120° C.
  • the average film thickness of the hardened film varies with the desired coating purpose, and generally ranges from 1 to 20 microns, and preferably ranges from 5 to 10 microns.
  • the surface coating composition of the present invention can be advantageously applied to a variety of products such as sunglass lenses made of transparent plastic material, light and heavy lenses, viewfinder lenses for cameras, other optical lenses, transparent covers for meters of a variety of measurement devices, window glass of an automobile, electric vehicle and airplane, and mirrors made of plastic material.
  • a mixture of 120 parts by weight of methyltriethoxysilane, 30 parts by weight of water and 5 ppm of hydrochloric acid was heated for 4 hours and 20 minutes, under stirring and refluxing. In the last period of the heating, water and the by-produced alcohol were removed by evaporation. The residue remaining after the evaporation was then heated at 140° C. for 1 minute.
  • a polymethylmethacrylate resin sheet (100 mm ⁇ 100 mm ⁇ 2 mm), and the sheet was then taken out of the solution at a rate of 20 cm/min. with no vibrating action.
  • the thus-treated sheet was immediately placed in a hot-air oven and heated at 90° C. for 10 hours to dry and harden the coated organopolysiloxane coating composition.
  • the thus-obtained coating sheet was evaluated in the following manner.
  • the surface of the coating sheet was subjected to abrasion in a Taber Abrasion Testing Device (prepared by Yasuda Seiki, Japan) under the conditions of a load of 500 g., 100 cycles, using the wheel of CS-10F.
  • the coating sheet was then measured in a Haze Meter (prepared by Suga Testing Machine Corp., Japan) to determine the total light transmittance and the scattered light.
  • the abrasion resistant property is expressed by the value of the haze as calculated below. ##EQU1##
  • a pair of sheets (60 mm ⁇ 60 mm) to be tested were placed one upon the other on a horizontal base.
  • the upper sheet was adhered to the weight.
  • One end of a string was tied to the center of one side of the weight and the other end was tied to the Tensile Testing Machine (manufactured by Toyo Seiki Corp., Japan). The string was pulled by the testing machine.
  • --Friction F(g) exerted by the Tensile Testing Machine to cause relative sliding of the sheets.
  • the direction of the string was altered from horizontal to vertical by introducing a pulley on the mid-portion of the string.
  • the friction was produced between the upper sheet and the lower sheet.
  • the surface friction resistance is calculated by the following equation.
  • the sheet was measured to determine the light transmittance by means of a color difference meter (Suga Testing Machine Corp.)
  • Example 1 The procedure described in Example 1 was repeated except that the fluorocarbon-type surface active agent was not incorporated. The results measured and observed on the tested sheet are set forth in Table 1.
  • Example 1 The methacrylic resin sheet employed in Example 1, per se (without the coating), was subjected to the same measurements and observations. The results measured and observed on the tested sheet are set forth in Table 1.
  • the sheet coated with the composition containing the fluorocarbon-type surface active agent is more excellent in the anti-abrasion property and the surface friction resistance compared with the sheet that was coated with the composition containing no fluorocarbon-type surface active agent (Comparative Example 1) and the sheet with no coating (Comparative Example 2).
  • the film obtained in Example 1 was transparent even though it contained the fluorocarbon-type surface active agent, and the fluorocarbon property of the coated film was satisfactory.
  • Example 1 The procedure described in Example 1 was repeated except that the surface active agent C 9 F 17 COONa was employed in place of the surface active agent C 9 F 17 OC 6 H 4 SO 3 Na employed in Example 1, and a coating solution was prepared.
  • the coating solution was dipped the polycarbonate sheet which had been provided with the under-coating layer, and the thus-treated sheet was immediately introduced into a hot-air oven and heated at 110° C. for 5 hours.
  • Ths thus-obtained coated sheet was evaluated in the same manner as described in Example 1. The results are set forth in Table 1. The properties of the coated film are substantially identical to those of the coated film prepared in Example 1.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)
US06/153,242 1979-06-06 1980-05-27 Surface coating composition Expired - Lifetime US4338375A (en)

Applications Claiming Priority (2)

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JP54-70740 1979-06-06
JP54070740A JPS6017380B2 (ja) 1979-06-06 1979-06-06 表面被覆用組成物

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GB (1) GB2051843B (sv)

Cited By (35)

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US4413025A (en) * 1980-11-12 1983-11-01 Daicel Chemical Industries, Ltd. Coating composition for polycarbonate moldings containing partially hydrolyzed alkyltrialkoxysilane and polyvinylbutyral
US4417790A (en) * 1979-05-10 1983-11-29 American Optical Corporation Finished ophthalmic lens comprising an optical smooth coating over a rough-surfaced base
US4455403A (en) * 1981-09-02 1984-06-19 Rohm Gmbh Silicone resin coating agent
US4472510A (en) * 1982-12-23 1984-09-18 Dow Corning Corporation Carbon-containing monolithic glasses and ceramics prepared by a sol-gel process
US4490495A (en) * 1982-11-15 1984-12-25 Techsight Corp. Composition and method for tinting plastic
US4540629A (en) * 1982-04-08 1985-09-10 Pq Corporation Hollow microspheres with organosilicon-silicate walls
USRE32107E (en) * 1982-12-23 1986-04-08 Dow Corning Corporation Carbon-containing monolithic glasses and ceramics prepared by a sol-gel process
US4711820A (en) * 1986-06-17 1987-12-08 Petrarch Systems Inc. Method of siliconization of surfaces with lower alkyl silanes
US4774035A (en) * 1986-01-14 1988-09-27 Camelot Industries Corporation Process of coating an ophthalmic lens
US4816049A (en) * 1985-07-12 1989-03-28 Hoya Corporation Process of surface treating laser glass
US4898755A (en) * 1987-04-17 1990-02-06 Hoechst Celanese Corporation Inorganic-organic composite compositions exhibiting nonlinear optical response
US4944962A (en) * 1987-10-24 1990-07-31 Ito Optical Industrial Co., Ltd. Method for dirtproofing treatment for plastic lens
WO1992006101A1 (en) * 1990-10-09 1992-04-16 Prosoco, Inc. Method of rendering masonry materials water repellent with low voc organoalkoxysilanes
US5152834A (en) * 1990-09-14 1992-10-06 Ncr Corporation Spin-on glass composition
US5162407A (en) * 1990-03-06 1992-11-10 Investors Diversified Capital, Inc. Silicone rubber sealant composition
USRE34584E (en) * 1984-11-09 1994-04-12 The Procter & Gamble Company Shampoo compositions
US5314947A (en) * 1990-06-11 1994-05-24 Nipon Arc Co., Ltd. Coating composition and article coated thereby
US5322888A (en) * 1991-06-25 1994-06-21 Itoh Optical Industrial Co., Ltd. Coating composition for optical plastic moldings
US5472488A (en) * 1990-09-14 1995-12-05 Hyundai Electronics America Coating solution for forming glassy layers
US5527931A (en) * 1992-03-20 1996-06-18 Minnesota Mining And Manufacturing Company Aqueous dispersable oil and water repellent silane masonry penetrants
US5527872A (en) * 1990-09-14 1996-06-18 At&T Global Information Solutions Company Electronic device with a spin-on glass dielectric layer
FR2774680A1 (fr) * 1998-02-10 1999-08-13 Essilor Int Procede de revetement d'un substrat en verre organique et solution de traitement
US6268089B1 (en) * 1998-02-23 2001-07-31 Agere Systems Guardian Corp. Photorecording medium and process for forming medium
WO2001064804A1 (en) * 2000-02-28 2001-09-07 Adsil, Lc Silane-based, coating compositions, coated articles obtained therefrom and methods of using same
US6358612B1 (en) 1997-08-27 2002-03-19 Bayer Aktiengesellschaft Coating compositions with a base consisting of silanes containing epoxide groups
US6361868B1 (en) 1997-08-28 2002-03-26 Bayer Aktiengesellschaft Coating compounds based on silanes containing epoxide groups
US6423770B1 (en) 1999-07-15 2002-07-23 Lucent Technologies Inc. Silicate material and process for fabricating silicate material
US6451382B2 (en) 2000-02-08 2002-09-17 John B. Schutt Method for improving heat efficiency using silane coatings and coated articles produced thereby
WO2002100151A2 (en) * 2000-02-28 2002-12-19 Adsil, Lc Non-aqueous coating compositions formed from silanes and metal alcoholates
US6572978B1 (en) * 1994-05-24 2003-06-03 Brian G. Bagley Method of making wood composition boards resistant to water permeation
DE20308885U1 (de) 2003-06-05 2003-08-14 Cofresco Frischhalteprodukte GmbH & Co. KG, 32427 Minden Beschichtungsmaterial, Beschichtung und Aluminiumfolie
KR100596968B1 (ko) 2005-03-17 2006-07-04 (주)피엠씨 콘크리트 침투성 흡수방지제용 수성실리콘 조성물의 제조방법
CN106661378A (zh) * 2014-07-30 2017-05-10 埃西勒国际通用光学公司 用于由热塑性聚丙烯酸酯制成的基底的防磨漆组合物
CN107001125A (zh) * 2014-11-28 2017-08-01 日本板硝子株式会社 带低反射涂层的玻璃板
US20180172884A1 (en) * 2014-07-03 2018-06-21 Essilor International (Compagnie Generale D'optique) Ophthalmic lens having different anti-fouling properties on each of the two surfaces thereof and manufacturing methods

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EP0075962A1 (de) * 1981-09-30 1983-04-06 Josef Dr. PÜHRINGER Imprägnierungsmittel für poröse Baumaterialien
JP2530436B2 (ja) * 1986-09-18 1996-09-04 住友化学工業株式会社 コ−テイング組成物
DE3781391D1 (de) * 1987-01-02 1992-10-01 Kaufmann Richard & Co Mittel zur verbesserung der hydrophoben eigenschaften von anorganischen materialien.
JPH0832854B2 (ja) * 1987-01-06 1996-03-29 日本合成ゴム株式会社 コ−テイング用組成物
JP2652169B2 (ja) * 1987-09-01 1997-09-10 大三工業株式会社 ガラス容器のかすれ傷塗布剤
FR2620719B1 (fr) * 1987-09-23 1994-06-03 Conseil Rech Etu Engineerin Compositions de revetement protecteur de surfaces non poreuses a base de polysiloxanes
DE4338361A1 (de) * 1993-11-10 1995-05-11 Inst Neue Mat Gemein Gmbh Verfahren zur Herstellung von Zusammensetzungen auf der Basis von Epoxidgruppen-haltigen Silanen
DE202018102849U1 (de) 2018-05-22 2018-05-30 Zipps Skiwachse Gmbh Gleitmittel für den Gebrauch auf Gleitflächen von Wintersportgeräten

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US3642880A (en) * 1966-03-24 1972-02-15 Allied Chem Novel polyfluorosulfonate salts
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US4173490A (en) * 1978-04-18 1979-11-06 American Optical Corporation Coating composition
US4275118A (en) * 1979-01-15 1981-06-23 Dow Corning Corporation Pigment-free coatings with improved resistance to weathering

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Patent Citations (5)

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Publication number Priority date Publication date Assignee Title
US3451838A (en) * 1965-12-03 1969-06-24 Owens Illinois Inc Process of coating plastics with organopolysiloxanes and articles made thereby
US3642880A (en) * 1966-03-24 1972-02-15 Allied Chem Novel polyfluorosulfonate salts
US4024306A (en) * 1974-03-25 1977-05-17 Shin-Etsu Chemical Company Limited Method of preparing an organopolysiloxane for surface coating
US4173490A (en) * 1978-04-18 1979-11-06 American Optical Corporation Coating composition
US4275118A (en) * 1979-01-15 1981-06-23 Dow Corning Corporation Pigment-free coatings with improved resistance to weathering

Cited By (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4417790A (en) * 1979-05-10 1983-11-29 American Optical Corporation Finished ophthalmic lens comprising an optical smooth coating over a rough-surfaced base
US4413025A (en) * 1980-11-12 1983-11-01 Daicel Chemical Industries, Ltd. Coating composition for polycarbonate moldings containing partially hydrolyzed alkyltrialkoxysilane and polyvinylbutyral
US4455403A (en) * 1981-09-02 1984-06-19 Rohm Gmbh Silicone resin coating agent
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JPS55164255A (en) 1980-12-20
JPS6017380B2 (ja) 1985-05-02
DE3021018C2 (sv) 1988-03-31
GB2051843B (en) 1983-08-10
GB2051843A (en) 1981-01-21
DE3021018A1 (de) 1980-12-18

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